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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 500538Generated: October 30, 2026

Diisopropylethylamine → 6-Oxo-1-(2-trimethylsilanyl-ethoxymethyl)-1,6-dihydro-pyridazine-4-carboxylic acid ethyl ester

https://huagongshe.com/reaction/500538

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
Reactant2-Chloromethyl 2-(trimethylsilyl)ethyl etherHCID 2724271—
ReactantEthyl 6-oxo-1,6-dihydropyridazine-4-carboxylateHCID 12376258—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
Product6-Oxo-1-(2-trimethylsilanyl-ethoxymethyl)-1,6-dihydro-pyridazine-4-carboxylic acid ethyl esterHCID 2485170253.2%

Reaction Conditions

Temperature0 °C

Reaction Steps

The title compound from Example 18.4 (0.90 g, 5.35 mmol) was stirred in dimethylformamide (20 mL) and diisopropyl ethylamine (1.39 mL, 8.025 mmol) at 0° C. and (2-chloromethoxy-ethyl)-trimethyl-silane (1.88 mL, 10.70 mmol) was added and the reaction was allowed to continue to stir at 0° C. for 2 hours and then overnight at r.t. The reaction mixture was diluted with EtOAc and washed with water and brine. The organic phase was dried over sodium sulfate, filtered and concentrated onto silica gel. The product was purified by column chromatography (0-20% EtOAc/hexanes) to afford the title compound as a clear oil (0.85 g, 53%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07772235B2
Source datasetuspto-grants-2010_08
ORD IDord-56de719ec7044f52a82a8837ab42c978
Source noteuspto-grants-2010_08